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ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data.
Çelik, Gökalp; Tuncali, Timur.
Affiliation
  • Çelik G; Health Sciences Institute, Department of Medical Genetics, Ankara Yildirim Beyazit University, Ankara, Turkey.
  • Tuncali T; Department of Medical Genetics, Ankara University School of Medicine, Ankara, Turkey.
Hum Mutat ; 43(2): 158-168, 2022 02.
Article in En | MEDLINE | ID: mdl-34923717
ABSTRACT
Runs of long homozygous (ROH) stretches are considered to be the result of consanguinity and usually contain recessive deleterious disease-causing mutations. Several algorithms have been developed to detect ROHs. Here, we developed a simple alternative strategy by examining X chromosome non-pseudoautosomal region to detect the ROHs from next-generation sequencing data utilizing the genotype probabilities and the hidden Markov model algorithm as a tool, namely ROHMM. It is implemented purely in java and contains both a command line and a graphical user interface. We tested ROHMM on simulated data as well as real population data from the 1000G Project and a clinical sample. Our results have shown that ROHMM can perform robustly producing highly accurate homozygosity estimations under all conditions thereby meeting and even exceeding the performance of its natural competitors.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Algorithms / High-Throughput Nucleotide Sequencing Type of study: Health_economic_evaluation Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: Turkey

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Algorithms / High-Throughput Nucleotide Sequencing Type of study: Health_economic_evaluation Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: Turkey